138330-03-7 Usage
General Description
2-(4-methoxyphenyl)-4-methylthiazole, also known as Anisole thiazole, is a chemical compound with the molecular formula C11H11NOS. It is a thiazole derivative with a methyl and a methoxy group attached to the thiazole ring. 2-(4-methoxyphenyl)-4-methylthiazole is commonly used as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. It has also been studied for its potential anti-cancer and anti-inflammatory properties. Additionally, it has applications in the fragrance industry due to its pleasant odor. However, it is important to handle this compound with care as it may pose health risks upon exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 138330-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138330-03:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*0)+(2*0)+(1*3)=107
107 % 10 = 7
So 138330-03-7 is a valid CAS Registry Number.
138330-03-7Relevant articles and documents
PdII-Catalyzed Regio- and Enantioselective Oxidative C?H/C?H Cross-Coupling Reaction between Ferrocenes and Azoles
Cai, Zhong-Jian,Liu, Chen-Xu,Gu, Qing,Zheng, Chao,You, Shu-Li
supporting information, p. 2149 - 2153 (2019/01/24)
Asymmetric C?H bond functionalization reaction is one of the most efficient and straightforward methods for the synthesis of optically active molecules. Herein we disclose an asymmetric C?H/C?H cross-coupling reaction of ferrocenes with azoles such as oxazoles and thiazoles. Palladium(II)/monoprotected amino acid (MPAA) catalytic system which exhibits excellent reactivity and regioselectivity for oxazoles and thiazoles. This method offers a powerful strategy for constructing planar chiral ferrocenes. Mechanistic studies suggest that the C?H bond cleavage of azoles is likely proceeding through a SEAr process and may not be a turnover limiting step.
